About AB Cube Germany
Innovating Clinical Trials
Since 2002
As part of the AB Cube Group, we deliver an integrated end-to-end eClinical ecosystem designed to support the evolving needs of clinical operations and clinical data management through a connected suite of innovative applications.
With more than 20 years of experience in EDC technology, our team combines deep expertise in clinical research, project management, software development, data privacy, and information security. We are committed to responsive collaboration, operational excellence, and supporting the success of every trial.
We believe that every day saved can make a difference.
Founded in Munich, Germany, Marvin was created with the vision of building a modern CDISC-native EDC platform that accelerates database development, streamlines study build processes, and reduces data management programming effort.
Fast Facts About AB Cube
25+ Years of Innovation
Pioneering EDC since 2002.
30+ Countries Served
A trusted global partner in pharmacovigilance, medical device vigilance, cosmetovigilance, and nutrivigilance.
10,000+ Trials conducted
Trials conducted across oncology, neurology, cardiology & rare disease
500+ Sites
Relationships with more than 500 oncology and cancer center sites globally
100% Cloud-Based
No local installation, no maintenance hassle.
AI enabler
Integration of future ready solutions enabled by AI with a strong focus on data safety and integrity
2002
XClinical was founded in Munich
2003
Marvin EDC
Launch of Marvin EDC
2007
Marvin 2.0 was one of the first EDC systems to be CDISC certified
2013
First oncology registry with sub-studies in Marvin
2020
Marvin EDC
Marvin 3.0 released
2023
ODSeasyNet
Asthenis software for documenting cancer cases joins with Marvin
2024
Marvin EDC
Release and onboarding of our Data Hub and Reporting Module “StudyMetrIQs”
2025
Study Designer (AI-enabled)
Release of first AI Use Cases
2026
Merger & Acquisition
Merger and acquistion with AB Cube. Integrating with Vigilance Suite from AB Cube SafetyEasy®
Why Marvin & AB Cube?
Compliance & Security by Design - Built on a robust, pre-validated framework aligned with global regulatory standards and requirements.
Full Compliance with GCP and 21 CFR Part 11 Standards
Our solutions ensure full compliance with Good Clinical Practice (GCP) and are designed to meet the requirements of major regulatory bodies (FDA, EMA, MHRA, PMDA, etc.).
GDPR-Compliant Data Handling and EU Data Storage
We securely host data within the EU, ensuring GDPR compliance for European academic institutions while protecting sensitive patient data with SSL encryption and enterprise-grade security standards.
Secure Audit Trails and Role-Based Access Control
Maintain detailed audit trails for full transparency and enforce role-based access control to ensure that only authorized personnel can access or modify sensitive clinical data.